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FDA 510(k)

YESNG MODEL 500SII ELECTROSURGICAL UNIT

K-Number: K880073 · 1988-03-11

ApplicantFerguson Medical
Decision Date1988-03-11
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

YESNG MODEL 500SII ELECTROSURGICAL UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1988-03-11 under 510(k) number K880073. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YESNG MODEL 500SII ELECTROSURGICAL UNIT?

YESNG MODEL 500SII ELECTROSURGICAL UNIT is a medical device that received FDA 510(k) clearance on 1988-03-11. The listed applicant is Ferguson Medical. The 510(k) number is K880073.

When did YESNG MODEL 500SII ELECTROSURGICAL UNIT receive FDA 510(k) clearance?

YESNG MODEL 500SII ELECTROSURGICAL UNIT received FDA 510(k) clearance on 1988-03-11, under 510(k) number K880073.

Who is the listed applicant for YESNG MODEL 500SII ELECTROSURGICAL UNIT?

The FDA 510(k) record lists Ferguson Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YESNG MODEL 500SII ELECTROSURGICAL UNIT?

The FDA product code for YESNG MODEL 500SII ELECTROSURGICAL UNIT is GEI.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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